Rms Co. (contract manufacturer, Minneapolis, MN): 9 new FDA device listings, incl. intervertebral fusion device with bone graft, lumbar

Rms Co. (Minneapolis, Minnesota): 9 new FDA device listings, incl. intervertebral fusion device with bone graft, lumbar. Its amount of 9 is top-decile (92nd percentile of 2,570 records). Dated 82 days ago, it serves as a historical benchmark. Score 80/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 9 · 92th percentile of 2,570 DeviceEstablishmentPulse records · 9.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 42 related MN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentRms Co.
Owner / operatorThe Cretex Companies, Inc.
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationMinneapolis, MN, US
New listings9
DevicesIntervertebral Fusion Device With Bone Graft, Lumbar; Intervertebral Fusion Device With Bone Graft, Thoracic; Intervertebral Fusion Device With Integrated Fixation, Lumbar; Intervertebral Fusion Device With Bone Graft, Cervical; Intervertebral Fusion Device With Integrated Fixation, Cervical
Product codesMAX, PHM, OVD, ODP, OVE
Device classesClass II
Medical specialtiesOrthopedic
Brand namesSymmetrix™ L Spinal System; CONDUIT™ ZERO-P™ VA Secured Spacer System
First new listing2026-07-10
Latest new listing2026-08-14
FDA registration number2183946
Registration expires2026-12-31
amount percentile92th of 2,570 (median 1, 9.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-08-14
  • Data refreshed: 2026-10-28
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Rms Co. and 43 Minnesota peers

  • Minnesota DeviceEstablishmentPulse records like this one: 43
  • Rms Co.'s amount: 92nd percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Minnesota peer: $8,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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80 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Rms Co. in Minneapolis, Minnesota?

Rms Co. (Minneapolis, MN), a contract manufacturer, added 9 FDA device listings between 2026-07-10 and 2026-08-14.

How does Rms Co. compare to other Minnesota DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 9 is 9.0x the median of 1 across 2,570 records. It is 82 days old; check the official source for later updates before acting. Its Score of 80/100 puts it among the stronger signals in this feed.

Rms Co. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Rms Co.Minneapolis, MN992nd2026-08-14
Arthrex, Inc.Ave Maria, FL1093rd2026-09-27
Biopro, Inc.Port Huron, MI1194th2026-10-15
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16

Related records

DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Minnesota

Cross-dataset signals in Minnesota

FdaApprovalPulse: records in Minnesota (61)

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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.

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